This is a phase 2 trial investigating the effect and safety of afatinib in previously treated recurrent or metastasic esophageal squamous cell carcinoma with EGFR overexpression or EGFR amplification.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Afatinib is orally administered at 40mg Qd of each 28 day cycle.
Peking University Cancer Hospital and Institute
Beijing, Beijing Municipality, China
Objective response rate
Percentage of patients who achieve partial response (PR) or complete response (CR) based on Response Evaluation Criteria In Solid Tumors (RECIST).
Time frame: From date of first dose until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.
Incidence of Treatment-Related Adverse Events
Number of adverse events of afatinib in patients with ESCC.
Time frame: Until 30 days after the last treatment
Disease control rate
Percentage of patients who achieve partial response (PR) or complete response (CR) or stable disease (SD) based on Response Evaluation Criteria In Solid Tumors (RECIST).
Time frame: From date of first dose until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months.
Progression free survival
Measure of time from study treatment to disease progression or death
Time frame: Up to 2 years
Overall survival
Measure of time from study treatment to patient's death or lost to follow-up.
Time frame: Up to 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.